HalolAt Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.Are You Ready to Create Your Own Sunshine?As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”Key responsibilities:
- Review and approval the QMS e.g OOS ,OOT, Lab event, deviations ,change control ,CAPA etc.
- Review /Approval the routine analytical raw data of finished products /API /IP/PV/Pkg etc.
- Assure all time readiness of site for regulatory agency inspectionsinternal audits and
appropriate implementation of corrective actions regarding observations made by theagenciesinternal audit teams.- Ensuring compliance to regulatory requirements on product, process and
release procedures. Ensure release of secure and effective drug products from site as per cGMPRequirement and regulatory commitment.- Facilitate internal and regulatory agency audits, ensuring that findings from site audits are
understood, assessed and addressed site wide in a comprehensive manner.- Monitor industry trends/issues faced internally and identify scope for improving Site quality
assurance management and processes.- Performs all work in support of our Corporate Values of Pride, Accountability, Integrity and
Diligence. Performs all work in accordance with all established regulatory and compliance andsafety requirements.- To ensure the compliance on control and maintenance of Quality Control system this includes
daily round and observati